Product Details

SNP ID
rs3731639
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.2:25734667 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GAATCCCTGATTAAACTTAATAAAA[G/T]TATTGACTCAAGTTGGTCTAATATA
Phenotype
MIM: 612991
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ASXL2 PubMed Links

Gene Details

Gene
ASXL2
Gene Name
additional sex combs like 2, transcriptional regulator
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018263.4 11298 Intron NP_060733.4
XM_006712039.3 11298 UTR 3 XP_006712102.1
XM_006712040.2 11298 UTR 3 XP_006712103.1
XM_011532950.2 11298 UTR 3 XP_011531252.1
XM_011532951.2 11298 UTR 3 XP_011531253.1
XM_017004429.1 11298 UTR 3 XP_016859918.1
XM_017004430.1 11298 UTR 3 XP_016859919.1

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